Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11199
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dc.contributor.authorPetronijević, Jelena-
dc.contributor.authorJanković, Nenad-
dc.contributor.authorStanojkovic, Tatjana-
dc.contributor.authorJoksimović N.-
dc.contributor.authorGrozdanic, Nadja-
dc.contributor.authorVranes, Milan-
dc.contributor.authorTot A.-
dc.contributor.authorBugarčić Z.-
dc.date.accessioned2021-04-20T17:44:34Z-
dc.date.available2021-04-20T17:44:34Z-
dc.date.issued2018-05-01-
dc.identifier.issn03656233-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11199-
dc.description.abstract© 2018 Deutsche Pharmazeutische Gesellschaft In order to investigate new potential therapeutically active agents, we investigated the biological properties of two small libraries of quinoxalinones and 1,4-benzoxazin-2-ones. The results obtained showed that compounds 5, 9–11 have good cytotoxic activity against HeLa cells where the lowest IC50 value (10.46 ± 0.82 μM/mL) was measured for compound 10. Additionally, the most active compounds (5, 9–11) showed much better selectivity for MRC-5 cells (up to 17.4) compared to cisplatin. In vitro evaluation of the inhibition of the enzyme α-glucosidase showed that compounds 10 and 11 exert significant inhibition of the enzyme at 52.54 ± 0.09 and 40.09 ± 0.49 μM, respectively. Competitive experiments with ethidium bromide (EB) indicated that all tested compounds have affinity to displace EB from the EB-DNA complex through intercalation, suggesting good competition with EB (Ksv = (3.1 ± 0.2), (5.1 ± 0.1), (5.6 ± 0.2), and (6.3 ± 0.2) × 103 M−1). A molecular docking study was also performed to better understand the binding modes and to conclude the structure–activity relationships of the synthesized compounds.-
dc.relation.ispartofArchiv der Pharmazie-
dc.titleBiological evaluation of selected 3,4-dihydro-2(1H)-quinoxalinones and 3,4-dihydro-1,4-benzoxazin-2-ones: Molecular docking study-
dc.typearticle-
dc.identifier.doi10.1002/ardp.201700308-
dc.identifier.scopus85045481725-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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